Canonical Allele Identifier: CA11380460
Gene: ZBTB38 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141375367G>A , CM000665.2:g.141375367G>A GRCh38
NC_000003.11:g.141094209G>A , CM000665.1:g.141094209G>A GRCh37
NC_000003.10:g.142576899G>A NCBI36
NG_021426.1:g.56155G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000321464.7:c.-235+5421G>A MANE Select ENSP00000372635.5:n.-235+5421G>A
ENST00000637706.1:n.436+5421G>A
ENST00000507657.1:n.390+5421G>A
ENST00000509842.5:c.-480+5421G>A ENSP00000426931.1:n.-480+5421G>A
ENST00000512276.5:n.556+5421G>A
ENST00000513619.5:n.576+5421G>A
NM_001080412.2:c.-480+5421G>A NP_001073881.2:n.-480+5421G>A
XM_024453431.1:c.-235+5421G>A XP_024309199.1:n.-235+5421G>A
XM_024453433.1:c.-480+5421G>A XP_024309201.1:n.-480+5421G>A
NM_001080412.3:c.-480+5421G>A NP_001073881.2:n.-480+5421G>A
NM_001376112.1:c.-235+5421G>A NP_001363041.1:n.-235+5421G>A
NM_001376113.1:c.-235+5421G>A MANE Select NP_001363042.1:n.-235+5421G>A
NM_001376114.1:c.-480+5421G>A NP_001363043.1:n.-480+5421G>A
NM_001376115.1:c.-172+5421G>A NP_001363044.1:n.-172+5421G>A
NM_001376116.1:c.-267+5421G>A NP_001363045.1:n.-267+5421G>A
NM_001376117.1:c.-333+5421G>A NP_001363046.1:n.-333+5421G>A
NM_001376118.1:c.-358+5421G>A NP_001363047.1:n.-358+5421G>A
NM_001376119.1:c.-106+5421G>A NP_001363048.1:n.-106+5421G>A
NM_001376120.1:c.-130+5421G>A NP_001363049.1:n.-130+5421G>A
NM_001376121.1:c.-636+5421G>A NP_001363050.1:n.-636+5421G>A
NM_001376122.1:c.-436+5421G>A NP_001363051.1:n.-436+5421G>A
NM_001376123.1:c.-603+5421G>A NP_001363052.1:n.-603+5421G>A
NM_001376124.1:c.-578+5421G>A NP_001363053.1:n.-578+5421G>A
NM_001387941.1:c.-333+5421G>A NP_001374870.1:n.-333+5421G>A
NM_001387945.1:c.-509+5421G>A NP_001374874.1:n.-509+5421G>A
NM_001387947.1:c.-1050+5421G>A NP_001374876.1:n.-1050+5421G>A
NM_001387948.1:c.-506+5421G>A NP_001374877.1:n.-506+5421G>A
NM_001387950.1:c.-423+5421G>A NP_001374879.1:n.-423+5421G>A
NM_001387952.1:c.-228+5421G>A NP_001374881.1:n.-228+5421G>A
NM_001387953.1:c.-285+5421G>A NP_001374882.1:n.-285+5421G>A
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